特發性間質性肺炎

特發性間質肺炎(Idiopathic interstitial pneumonia,簡稱IIP),又稱非感染性肺炎(noninfectious pneumonia)[1],屬於一種間質性肺病。該疾病通常侵襲肺間質,有些也會侵襲氣道(例如Cryptogenic organizing pneumonitis),IIP可分為七個亞型。

特發性間質性肺炎
Idiopathic interstitial pneumonia
Micrograph of usual interstitial pneumonia (UIP). UIP is the most common pattern of idiopathic interstitial pneumonia and usually represents 特发性肺纤维化. 苏木精-伊红染色. 驗屍 specimen.
症状肺炎
类型肺炎, 間質性肺病, 特發性
分类和外部资源
醫學專科胸腔醫學
Orphanet98300

組織學分類

IIP的分類相當複雜[2],須結合臨床觀察影像學,以及病理学[3][4]才能確診。

特發性間質性肺炎可由組織學型態分為下列數種[5][6]

組織學 臨床相關意義
Desquamative interstitial pneumonia (DIP) DIP
Diffuse alveolar damage (DAD) 急性呼吸窘迫症候群急性間質性肺炎輸血相關急性肺損傷
非特異性間質性肺炎(NSIP) NSIP
Respiratory bronchiolitis 呼吸性細支氣管相關之間質性肺病(RB-ILD)
尋常性間質性肺炎 (UIP) 自體免疫性疾病特发性肺纤维化致死量肺塵病
Organizing pneumonia 隱源性機化性肺炎
淋巴樣間質性肺炎 (LIP) LIP

其中尋常性間質性肺炎為最常見的一種亞型[7]

發育

Table 1: Development of the (histologic) idiopathic interstitial pneumonia classification

 
 
 
Leibow et al. (1969)
 
Katzenstein (1998)[8]
 
ATS/ERS (2002)[6]
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
UIP
 
UIP
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
UIP
 
 
DAD
 
DAD
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
NSIP
 
NSIP
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
DIP
 
DIP/RB
 
DIP
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
RB
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
BIP
 
OP
 
OP
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
LIP
 
(LPD)
 
LIP
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
GIP
 
(HMF)
 
(HMF)
 
 

UIP=usual interstitial pneumonia; DAD=diffuse alveolar damage; NSIP=non-specific interstitial pneumonia; DIP=desquamative interstitial pneumonia; RB=respiratory bronchiolitis; BIP=bronchiolitis obliterans interstitial pneumonia; OP=organizing pneumonia; LIP=lymphoid interstitial pneumonia; LPD=lymphoproliferative disease (not considered a diffuse lung disease); GIP=giant cell interstitial pneumonia; HMF=heavy metal fibrosis, no longer grouped with diffuse lung disease

Lymphoid interstitial pneumonia was originally included in this category, then excluded, then included again.[9]

參考文獻

  1. . New York, NY [u.a.]: Oxford Univ. Press. 1999: 833. ISBN 978-0-19-508103-9. Authors list列表中的|first1=缺少|last1= (帮助)
  2. Nicholson AG. . Histopathology. November 2002, 41 (5): 381–91. PMID 12405906. doi:10.1046/j.1365-2559.2002.01421.x.
  3. Flaherty KR, King TE, Raghu G, 等. . Am. J. Respir. Crit. Care Med. October 2004, 170 (8): 904–10. PMID 15256390. doi:10.1164/rccm.200402-147OC.
  4. Kim DS, Collard HR, King TE. . Proc Am Thorac Soc. June 2006, 3 (4): 285–92. PMC 2658683. PMID 16738191. doi:10.1513/pats.200601-005TK.
  5. Leslie KO, Wick MR. Practical Pulmonary Pathology: A Diagnostic Approach. Elsevier Inc. 2005. ISBN 978-0-443-06631-3.
  6. American Thoracic, Society; European Respiratory, Society. . Am. J. Respir. Crit. Care Med. January 2002, 165 (2): 277–304. PMID 11790668. doi:10.1164/ajrccm.165.2.ats01.
  7. Visscher DW, Myers JL. . Proc Am Thorac Soc. June 2006, 3 (4): 322–9 [2016-05-15]. PMID 16738196. doi:10.1513/pats.200602-019TK. (原始内容存档于2019-12-11).
  8. Katzenstein AL, Myers JL. . Am. J. Respir. Crit. Care Med. 1998, 157 (4 Pt 1): 1301–15. PMID 9563754. doi:10.1164/ajrccm.157.4.9707039.
  9. Swigris JJ, Berry GJ, Raffin TA, Kuschner WG. . Chest. December 2002, 122 (6): 2150–64. PMID 12475860. doi:10.1378/chest.122.6.2150.
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